PFM PROFESSIONAL 7000 SPIROMETER

PFM PROFESSIONAL 7000 SPIROMETER is an FDA 510(k)-cleared medical device (K932278) manufactured by Advanced Medical Systems, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 16, 1993. Regulation: 8.